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- ...and project management teams to ensure trials comply with Good Clinical Practice (GCP) and regulatory requirements. Work with pharmacovigilance teams to ensure timely and accurate safety reporting and management of safety signals during the trial. Represent Medical...SuggestedFull timeWork at officeWorldwide
- ...You are: ~ Bachelor’s degree in health science. Commensurate experience will be considered. ~5+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management required, and 4 years coding experience. ~ Expertise in medical...SuggestedRemote jobPermanent employment
- ...to Health Canada, Med Info, and enterinto source system and third-party systems. • Report and document Adverse Events as per Pharmacovigilance requirements. • Participate in quality activities and continuous improvement initiatives in keeping with thecompany’s Quality...SuggestedContract workLocal areaRemote workWork from homeHome office
